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Primary Resection and Immediate Autologous Reconstruction of Fronto-orbital Infantile Myofibromatoses

Infantile myofibromatosis is an unusual and rare lesion of the bone and soft tissue, which can be seen in the craniofacial skeleton. These complex tumors present a challenge to craniofacial surgeons regarding diagnosis, management, and safe and effective surgical treatment, frequently requiring comp...

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Autores principales: Lavie, Jennifer L., Rogers, Camille L., Stalder, Mark W., St. Hilaire, Hugo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7858576/
https://www.ncbi.nlm.nih.gov/pubmed/33552804
http://dx.doi.org/10.1097/GOX.0000000000003261
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author Lavie, Jennifer L.
Rogers, Camille L.
Stalder, Mark W.
St. Hilaire, Hugo
author_facet Lavie, Jennifer L.
Rogers, Camille L.
Stalder, Mark W.
St. Hilaire, Hugo
author_sort Lavie, Jennifer L.
collection PubMed
description Infantile myofibromatosis is an unusual and rare lesion of the bone and soft tissue, which can be seen in the craniofacial skeleton. These complex tumors present a challenge to craniofacial surgeons regarding diagnosis, management, and safe and effective surgical treatment, frequently requiring complex reconstruction. We present the case of a 7-month-old girl with multicentric infantile myofibromatosis of the right parietal and fronto-orbital region, the associated clinical presentation, histopathologic findings, and surgical management, along with a review of the relevant literature.
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spelling pubmed-78585762021-02-05 Primary Resection and Immediate Autologous Reconstruction of Fronto-orbital Infantile Myofibromatoses Lavie, Jennifer L. Rogers, Camille L. Stalder, Mark W. St. Hilaire, Hugo Plast Reconstr Surg Glob Open Pediatric/Craniofacial Infantile myofibromatosis is an unusual and rare lesion of the bone and soft tissue, which can be seen in the craniofacial skeleton. These complex tumors present a challenge to craniofacial surgeons regarding diagnosis, management, and safe and effective surgical treatment, frequently requiring complex reconstruction. We present the case of a 7-month-old girl with multicentric infantile myofibromatosis of the right parietal and fronto-orbital region, the associated clinical presentation, histopathologic findings, and surgical management, along with a review of the relevant literature. Lippincott Williams & Wilkins 2021-01-22 /pmc/articles/PMC7858576/ /pubmed/33552804 http://dx.doi.org/10.1097/GOX.0000000000003261 Text en Copyright © 2021 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Pediatric/Craniofacial
Lavie, Jennifer L.
Rogers, Camille L.
Stalder, Mark W.
St. Hilaire, Hugo
Primary Resection and Immediate Autologous Reconstruction of Fronto-orbital Infantile Myofibromatoses
title Primary Resection and Immediate Autologous Reconstruction of Fronto-orbital Infantile Myofibromatoses
title_full Primary Resection and Immediate Autologous Reconstruction of Fronto-orbital Infantile Myofibromatoses
title_fullStr Primary Resection and Immediate Autologous Reconstruction of Fronto-orbital Infantile Myofibromatoses
title_full_unstemmed Primary Resection and Immediate Autologous Reconstruction of Fronto-orbital Infantile Myofibromatoses
title_short Primary Resection and Immediate Autologous Reconstruction of Fronto-orbital Infantile Myofibromatoses
title_sort primary resection and immediate autologous reconstruction of fronto-orbital infantile myofibromatoses
topic Pediatric/Craniofacial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7858576/
https://www.ncbi.nlm.nih.gov/pubmed/33552804
http://dx.doi.org/10.1097/GOX.0000000000003261
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